Application of the polyvalent approach to HIV-1 vaccine development.

Julia L Hurwitz, Karen S Slobod, Tim D Lockey, Shixia Wang, Te-Hui W Chou, Shan Lu
{"title":"Application of the polyvalent approach to HIV-1 vaccine development.","authors":"Julia L Hurwitz,&nbsp;Karen S Slobod,&nbsp;Tim D Lockey,&nbsp;Shixia Wang,&nbsp;Te-Hui W Chou,&nbsp;Shan Lu","doi":"10.2174/1568005054201517","DOIUrl":null,"url":null,"abstract":"<p><p>One major obstacle to the design of a global HIV-1 vaccine is viral diversity. Presently, data suggest that a single antigen will not suffice to generate broadly reactive neutralizing antibodies to protect all individuals against all subtypes of HIV-1 infection. While some of the neutralizing epitopes are identified in the constant regions of the HIV-1 envelope (Env) glycoprotein, many are localized to variable regions and differ conformationally from one virus to the next. The successes of polyvalent vaccine approaches against other antigenically variable pathogens encourage adoption of the same approach for HIV-1 vaccine design. The critical question is which envelope antigens should be combined in a vaccine cocktail to provide maximum protection against HIV-1. A review of the existing human vaccines based on the polyvalent principle is included here to provide a historical perspective for the current effort of developing a polyvalent HIV-1 vaccine. Data generated from several groups actively working on candidate polyvalent HIV-1 vaccines are summarized. Information presented in this review highlights the potential and importance of the polyvalent vaccine approach for the future development of an effective HIV-1 vaccine.</p>","PeriodicalId":84525,"journal":{"name":"Current drug targets. Infectious disorders","volume":"5 2","pages":"143-56"},"PeriodicalIF":0.0000,"publicationDate":"2005-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2174/1568005054201517","citationCount":"35","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current drug targets. Infectious disorders","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/1568005054201517","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 35

Abstract

One major obstacle to the design of a global HIV-1 vaccine is viral diversity. Presently, data suggest that a single antigen will not suffice to generate broadly reactive neutralizing antibodies to protect all individuals against all subtypes of HIV-1 infection. While some of the neutralizing epitopes are identified in the constant regions of the HIV-1 envelope (Env) glycoprotein, many are localized to variable regions and differ conformationally from one virus to the next. The successes of polyvalent vaccine approaches against other antigenically variable pathogens encourage adoption of the same approach for HIV-1 vaccine design. The critical question is which envelope antigens should be combined in a vaccine cocktail to provide maximum protection against HIV-1. A review of the existing human vaccines based on the polyvalent principle is included here to provide a historical perspective for the current effort of developing a polyvalent HIV-1 vaccine. Data generated from several groups actively working on candidate polyvalent HIV-1 vaccines are summarized. Information presented in this review highlights the potential and importance of the polyvalent vaccine approach for the future development of an effective HIV-1 vaccine.

多价方法在HIV-1疫苗研制中的应用
设计全球HIV-1疫苗的一个主要障碍是病毒的多样性。目前的数据表明,单一抗原不足以产生广泛反应性中和抗体,以保护所有个体免受所有亚型HIV-1感染。虽然在HIV-1包膜(Env)糖蛋白的恒定区域发现了一些中和性表位,但许多表位定位于可变区域,并且不同病毒的构象不同。针对其他抗原性可变病原体的多价疫苗方法的成功,鼓励在HIV-1疫苗设计中采用相同的方法。关键的问题是,哪种包膜抗原应该结合在鸡尾酒疫苗中,以提供对HIV-1的最大保护。本文综述了基于多价原理的现有人用疫苗,为目前研制多价HIV-1疫苗的工作提供了历史视角。总结了几个积极研究候选多价HIV-1疫苗的小组所产生的数据。本综述中提出的信息强调了多价疫苗方法对未来开发有效的HIV-1疫苗的潜力和重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信